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Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism

The Zhuanggu Guanjie herbal formula has been a famous Chinese prescription for treating bone diseases since time immemorial. The anti-osteoarthritis (OA) properties of this botanical prescription are well documented in the Chinese Pharmacopoeia. However, the detailed mechanisms behind the phenomenon...

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Autores principales: Guowei, Gong, Yuzhong, Zheng, Xuan, Zhou, Zhi, Dai, Juanhui, Duan, Jing, Wang, Peikui, Yang, Xiangzhi, Liu, Zhen, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751418/
https://www.ncbi.nlm.nih.gov/pubmed/36532734
http://dx.doi.org/10.3389/fphar.2022.896397
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author Guowei, Gong
Yuzhong, Zheng
Xuan, Zhou
Zhi, Dai
Juanhui, Duan
Jing, Wang
Peikui, Yang
Xiangzhi, Liu
Zhen, Wen
author_facet Guowei, Gong
Yuzhong, Zheng
Xuan, Zhou
Zhi, Dai
Juanhui, Duan
Jing, Wang
Peikui, Yang
Xiangzhi, Liu
Zhen, Wen
author_sort Guowei, Gong
collection PubMed
description The Zhuanggu Guanjie herbal formula has been a famous Chinese prescription for treating bone diseases since time immemorial. The anti-osteoarthritis (OA) properties of this botanical prescription are well documented in the Chinese Pharmacopoeia. However, the detailed mechanisms behind the phenomenon have not been elucidated. Hence, we aimed to investigate the anti-OA efficacy of the Zhuanggu Guanjie herbal formula and its underlying mechanism. The anti-OA properties of Zhuanggu Guanjie capsule (ZGC) were determined by the cytokine contents and inflammatory-related proteins, which were measured by RT-PCR, flow cytometry, Western blot, and laser confocal assay in ATDC5 cells. The levels of interleukin-6, tumor necrosis factor-α, inducible nitric oxide synthase, cyclooxygenase-2, and prostaglandin synthesis E2 have been markedly reduced after being treated with ZGC for 48 h in a dose-dependent manner. Furthermore, ZGC prevented the translocation of NF-κB from the cytosol to the nucleus. On the other hand, we used the mono-iodoacetate (MIA)-induced OA model to confirm the in vivo efficacies of this herbal formula. Oral administration of ZGC attenuated MIA-induced OA damage through changes in histopathological and knee joint volumes. The serum matrix metalloproteinase-13 contents in the ZGC treatment group declined as compared to those in the MIA model group. Through our in vitro and in vivo studies, we confirmed the anti-OA efficacy of ZGC and uncovered its detailed mechanism, and this treatment shed light on OA pathophysiology.
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spelling pubmed-97514182022-12-16 Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism Guowei, Gong Yuzhong, Zheng Xuan, Zhou Zhi, Dai Juanhui, Duan Jing, Wang Peikui, Yang Xiangzhi, Liu Zhen, Wen Front Pharmacol Pharmacology The Zhuanggu Guanjie herbal formula has been a famous Chinese prescription for treating bone diseases since time immemorial. The anti-osteoarthritis (OA) properties of this botanical prescription are well documented in the Chinese Pharmacopoeia. However, the detailed mechanisms behind the phenomenon have not been elucidated. Hence, we aimed to investigate the anti-OA efficacy of the Zhuanggu Guanjie herbal formula and its underlying mechanism. The anti-OA properties of Zhuanggu Guanjie capsule (ZGC) were determined by the cytokine contents and inflammatory-related proteins, which were measured by RT-PCR, flow cytometry, Western blot, and laser confocal assay in ATDC5 cells. The levels of interleukin-6, tumor necrosis factor-α, inducible nitric oxide synthase, cyclooxygenase-2, and prostaglandin synthesis E2 have been markedly reduced after being treated with ZGC for 48 h in a dose-dependent manner. Furthermore, ZGC prevented the translocation of NF-κB from the cytosol to the nucleus. On the other hand, we used the mono-iodoacetate (MIA)-induced OA model to confirm the in vivo efficacies of this herbal formula. Oral administration of ZGC attenuated MIA-induced OA damage through changes in histopathological and knee joint volumes. The serum matrix metalloproteinase-13 contents in the ZGC treatment group declined as compared to those in the MIA model group. Through our in vitro and in vivo studies, we confirmed the anti-OA efficacy of ZGC and uncovered its detailed mechanism, and this treatment shed light on OA pathophysiology. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9751418/ /pubmed/36532734 http://dx.doi.org/10.3389/fphar.2022.896397 Text en Copyright © 2022 Guowei, Yuzhong, Xuan, Zhi, Juanhui, Jing, Peikui, Xiangzhi and Zhen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Guowei, Gong
Yuzhong, Zheng
Xuan, Zhou
Zhi, Dai
Juanhui, Duan
Jing, Wang
Peikui, Yang
Xiangzhi, Liu
Zhen, Wen
Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title_full Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title_fullStr Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title_full_unstemmed Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title_short Zhuanggu Guanjie herbal formula mitigates osteoarthritis via the NF-κB transduction mechanism
title_sort zhuanggu guanjie herbal formula mitigates osteoarthritis via the nf-κb transduction mechanism
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751418/
https://www.ncbi.nlm.nih.gov/pubmed/36532734
http://dx.doi.org/10.3389/fphar.2022.896397
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